51. Three new bis-trinorcadalenes from Decaschistia intermedia Craib and their α-glucosidase inhibitory activities
- Author
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Hoang Viet Dung, Nghiem Duc Trong, Duong Thi Dung, Nguyen Xuan Nhiem, Trinh Nam Trung, Nguyen Tuan Anh, Do Quyen, Bui Huu Tai, Phan Van Kiem, and Do Thi Thao
- Subjects
010405 organic chemistry ,Stereochemistry ,Plant Science ,01 natural sciences ,Biochemistry ,0104 chemical sciences ,010404 medicinal & biomolecular chemistry ,chemistry.chemical_compound ,chemistry ,Scopoletin ,Decaschistia ,Ic50 values ,Radix ,Scopolin ,Agronomy and Crop Science ,α glucosidase inhibitory ,Two-dimensional nuclear magnetic resonance spectroscopy ,Biotechnology - Abstract
Three new bis-trinorcadalenes, bistrinorcadintermes A–C (1-3) along with seven known compounds, parvifloral D (4), parvifloral E (5), parvifloral C (6), hymexelsin (7), scopoletin (8), scopolin (9), and hibiscolactone A (10) were isolated from the aerial parts and radix of Decaschistia intermedia Craib. Their chemical structures were determined based on spectroscopic methods, including 1D, 2D NMR, MS, and experimental CD spectra. All compounds were evaluated for their α-glucosidase inhibitory effects. Compounds 1, 5, and 8 showed moderate α-glucosidase inhibitory activities with IC50 values of 45.6 ± 4.2, 43.7 ± 3.6, and 43.7 ± 3.6 μg/mL, respectively. Compounds 2-4 and 10 showed weak α-glucosidase inhibitory activities with IC50 values ranging from 87.5 ± 6.3 to 219.8 ± 4.9 μg/mL.
- Published
- 2021